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临床试验/NCT06415552
NCT06415552尚未招募不适用

Implementation of Online Mindfulness-Based Stress Reduction Tailored for People with Multiple Sclerosis

Robert Simpson1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
120
试验地点
1
主要终点
Adherence

研究概览

简要总结

This project aims to implement and investigate a mindfulness-based stress reduction (MBSR) in people with multiple sclerosis (PwMS). The main objective is to implement MBSR intervention for PwMS in a major tertiary care clinic for PwMS. We will iteratively refine the intervention as required based on stakeholder feedback and any other emergent contextual findings.

Participants will be asked to take part in an 8-week MBSR course and report changes in anxiety, depression, quality of life, emotional regulation, self-compassion, mindfulness, and health services use.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Age >18 years </= 60 years
  • Diagnosis of MS or related condition (Clinically Isolated Syndrome, Neuromyelitis Optica Spectrum Disorder, Chronic Inflammatory Demyelinating Neuropathy)
  • Able to understand spoken and written English
  • Willing to take part in an MBSR course

排除标准

  • Cognitive impairment (<26 on the Montreal Cognitive Assessment)
  • Severe active mental health impairment (psychosis, suicidality)
  • Medical instability (terminal/life threatening inter-current illness)

结局指标

主要结局

Adherence

时间窗: 24 months

The investigators will measure the number of participants who completed the mindfulness-based stress reduction course.

Recruitment

时间窗: 24 months

The investigators will measure the number of participants eligible for and recruited to the study.

Retention

时间窗: 24 months

The investigators will measure the percentage of participants who complete outcome data.

Follow-up rates

时间窗: 24 months

The investigators will measure the percentage of participants who complete outcome measures pre-intervention, post-intervention, and at 3 months post-intervention.

次要结局

  • Quality of Life using the Multiple Sclerosis Impact Scale (MSIS-29)(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Anxiety(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Sleep(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Pain Effects(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Quality of Life using the EuroQol (EQ-5D-5L)(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Health services use(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Self-compassion(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Depression(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Emotion regulation(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Mindfulness(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Climate(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Therapeutic alliance(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Fatigue(Measured at baseline, 8-week follow-up, and 3-month follow-up)
  • Cognitive function(Measured at baseline, 8-week follow-up, and 3-month follow-up)

研究者

发起方
Robert Simpson
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Robert Simpson

Investigator

Unity Health Toronto

研究点 (1)

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